Vallee R
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3206-10. doi: 10.1073/pnas.77.6.3206.
Chymotryptic fragments of microtubule-associated protein 2 (MAP 2) containing the portion of the molecule responsible for promoting microtubule assembly were identified. These assembly-promoting fragments displaced intact MAP 2, but not MAP 1, from assembled microtubules. This indicates that the association of MAP 2 with the microtubule surface is reversible. Both the assembly-promoting fragments and fragments representing the portion of the MAP 2 molecule observed as a projection on the microtubule surface were found to contain sites for endogenous cyclic AMP-dependent phosphorylation. The projection fragments were capable of endogenous phosphorylation even after their physical separation from microtubules. This suggests an intimate association of a kinase activity with the projections. Detailed analysis of the properties of the chymotryptic fragments of MAP 2 has led to a map of the molecule showing the major sites of proteolytic attack and the sites of phosphorylation.
已鉴定出微管相关蛋白2(MAP 2)的胰凝乳蛋白酶片段,其包含分子中负责促进微管组装的部分。这些促进组装的片段从组装好的微管上取代了完整的MAP 2,但没有取代MAP 1。这表明MAP 2与微管表面的结合是可逆的。促进组装的片段以及在微管表面呈突起状观察到的代表MAP 2分子部分的片段都被发现含有内源性环磷酸腺苷依赖性磷酸化位点。即使在与微管物理分离后,突起片段仍能够进行内源性磷酸化。这表明激酶活性与突起之间存在密切关联。对MAP 2胰凝乳蛋白酶片段性质的详细分析已得出该分子的图谱,显示了蛋白水解攻击的主要位点和磷酸化位点。